Cargando…
Severe congenital neutropenia, a genetically heterogeneous disease group with an increased risk of AML/MDS
Over the past decade, enormous progress has been made in the understanding of severe congenital neutropenia (SCN), by identification of several causal gene mutations: in ELANE, GFI1, HAX1, WAS and G3PC3. SCN is a preleukemic condition, independent of the genetic subtype. Acquired CSF3R mutations are...
| Autores principales: | , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
PAGEPress Publications
2011
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206537/ https://www.ncbi.nlm.nih.gov/pubmed/22053285 http://dx.doi.org/10.4081/pr.2011.s2.e9 |